Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001024611.2 | 3902 | Missense Mutation | AAC,AGC | N723S | NP_001019782.1 |
XM_011534383.2 | 3902 | Missense Mutation | AAC,AGC | N775S | XP_011532685.1 |
XM_017008162.1 | 3902 | Missense Mutation | AAC,AGC | N487S | XP_016863651.1 |